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FDA 510(k)

PIN PUNCH

K-Number: K874356 · 1987-11-23

Decision Date1987-11-23
Product CodeLRY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PIN PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tool, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K874356. The device is classified under product code LRY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIN PUNCH?

PIN PUNCH is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Med-Tool, Inc.. The 510(k) number is K874356.

When did PIN PUNCH receive FDA 510(k) clearance?

PIN PUNCH received FDA 510(k) clearance on 1987-11-23, under 510(k) number K874356.

Who is the listed applicant for PIN PUNCH?

The FDA 510(k) record lists Med-Tool, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIN PUNCH?

The FDA product code for PIN PUNCH is LRY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Med-Tool, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 28 devices →

Related Devices (Code: LRY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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